Associate Research Manager Job at Kantar (Manila)

Clinical Research Associate II/Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Must be fluent in English and in the native language(s) of the country they will work in
Ability to travel 60-80%
Valid driver’s license and passport required
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
Serve as the primary point of contact for assigned investigator sites
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel
Attend investigator meeting when required
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit
Submit all required reports, documentation, updates and tracking within required timeframes
Identify and resolve investigator site issues within required timeframes

What we offer

Career growth and development
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Clinical Research Associate II / Senior Clinical Research Associate Large Pharma

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Germany , Frankfurt

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Master or Bachelor's degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
Excellent communication skills in German and English
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Job Responsibility

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Senior Associate, Project Manager Market Research Operations

This is an exciting opportunity for a project management professional to join th...

Location

United States , McLean; New York

Salary:

96500.00 - 120100.00 USD / Year

Capital One

Expiration Date

Until further notice

Requirements

Bachelor's Degree or Military experience
At least 3 years of Program or Project Management experience
At least 3 years of experience utilizing Scrum, Kanban or SAFe methodologies
At least 2 years of Relationship management experience

Job Responsibility

Lead and manage recurring team level operations including core research program studies and enterprise governance standards
Research program management including maintaining & updating our primary research project tracker and overall research calendar management
Budget management ensuring accurate tracking of research project spend in partnership with finance team support
Vendor management liaising with primary and secondary research vendors
Coordinate recurring team level communications including socializing team capabilities, research studies, creating newsletters, and sharing project pipeline updates

What we offer

Performance based incentive compensation which may include cash bonus(es) and/or long term incentives (LTI)
Comprehensive, competitive, and inclusive set of health, financial and other benefits

Fulltime

Research Associate - Content Focused Project Manager

Harvard Business School seeks a Research Associate (RA) to support a faculty mem...

Location

United States , Boston

Salary:

Not provided

HBS

Expiration Date

Until further notice

Requirements

Bachelor’s degree in business or a related field (a GPA above 3.5 is required)
Proven writing experience
Prior experience supporting short form writing and website project management preferred
Evidence of prior high-quality, original academic writing
Background in analysis and interpretation of relevant data, research, news, and literature
Ability to read academic, subject-specific information and write a reasoned and thoughtful analysis, as well as produce a creative interpretation
Extremely high standards in terms of quality of work, attention to detail, strong organization skills, and absolute commitment to task completion
Ability to balance multiple tasks and shifting priorities under tight deadlines at an accelerated pace when necessary
Familiarity with navigating a complex organization, such as Harvard Business School

Job Responsibility

Build trust and collaboration by being present on-site and engaging directly with colleagues and various constituents
Work under the general direction of HBS faculty on topics central to HBS research agenda
Provide subject-area knowledge, analysis and interpretation to faculty member
Identify and explore a wide-range of questions related to faculty’s research agenda
Write cases, case supplements, project reports, and drafts for a book project from start to finish creating original writing based on subject-area expertise, research, and interviews
Write articles for applicable business audiences such as Harvard Business Review
Under general direction of faculty member, must be able to take complex research ideas, concepts, and methodologies and apply them to new projects and situations
Must be able to structure assignments and keep faculty member informed as necessary, using own judgment
Responsible for other duties as assigned

What we offer

Generous paid time off including parental leave
Medical, dental, and vision health insurance coverage starting on day one
Retirement plans with university contributions
Wellbeing and mental health resources
Support for families and caregivers
Professional development opportunities including tuition assistance and reimbursement
Commuter benefits, discounts and campus perks

Parttime

Associate Project Manager, Center for Artificial Intelligence Research

Under general direction, the Associate Project Manager provides administrative a...

Location

United States , Winston Salem

Salary:

28.55 - 42.85 USD / Hour

Advocate Aurora Health

Expiration Date

Until further notice

Requirements

Bachelor's degree in Education, Public Health, Basic Science, or a relevant clinical discipline with two years survey research experience including interviewing, supervision of data collection procedures, and training
community event planning
or, an equivalent combination of education and experience
Master's degree in a relevant discipline preferred
Ability to provide direction to research staff
Excellent oral, written, and interpersonal communication skills
Knowledge of computerized data processing and statistical analysis
Demonstrates knowledge of scientific principles

Job Responsibility

Provides administrative and coordination support for the design, implementation, and evaluation of projects and programs
Coordinates day-to-day project activities, managing timelines and communications
Maintains the Director’s calendar and scheduling
Assists with reporting and documentation
Supports recruitment, onboarding, and engagement activities for students, staff, and collaborators
Helps organize research and educational events such as seminars, workshops, and the annual colloquium
Responsible for the planning, development, implementation and evaluation of certain phases of the assigned project(s)
Translates planning and design decisions into concrete activities and tasks to be undertaken and set priorities as appropriate
Responsible for the administration and coordination of various aspects of the study
Responsible for ensuring that aspects of the study are conducted in accordance with the study protocol

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program

Fulltime

Research Associate - Ethnographic Research

Harvard Business School seeks a dedicated, enterprising, and collaborative Resea...

Location

United States , Boston

Salary:

Not provided

HBS

Expiration Date

Until further notice

Requirements

Bachelor’s degree required
Evidence of outstanding academic achievement
Indication of independent research experience, project management, and/or related applied experience
Strong skills related to the Microsoft Office Suite are expected
Excellent writing, editing, research skills
Analytically-minded and possess strong conceptual skills
Strong people, project-management, and organizational skills
Proven ability to handle multiple projects simultaneously and to flexibly adapt to changes in priorities
Ability to work calmly under deadline pressure, work both independently and as a team member, take initiative
and follow projects through to completion

Job Responsibility

Conduct field and ethnographic research
Conduct newspaper research, literature reviews, and library searches
Engaging in project management
Write draft cases and articles, case supplements, project reports, and policy memos creating original writing based on research and interviews
Provide analysis, editing, and drafts for academic journal articles, HBS cases and HBS teaching notes
Develop, synthesize and provide analysis of literature reviews
Independently manage all timelines and deliverables for multiple projects with competing priorities
Exercise independent decision making with regard to progression of research project and methodologies
Must be able to structure assignments and keep faculty member informed regularly while using own judgment
Build trust and collaboration by being present on-site and engaging directly with colleagues and various constituents

What we offer

Generous paid time off including parental leave
Medical, dental, and vision health insurance coverage starting on day one
Retirement plans with university contributions
Wellbeing and mental health resources
Support for families and caregivers
Professional development opportunities including tuition assistance and reimbursement
Commuter benefits, discounts and campus perks

Fulltime

Associate Manager / Manager - MedTech Healthcare

A fantastic opportunity for an experienced candidate to join this global market ...

Location

United States

Salary:

Not provided

Myn

Expiration Date

Until further notice

Requirements

Project Management: Strong ability to manage multiple workstreams in a fast-paced environment
Analytical Skills: Excellent quantitative and problem-solving skills with strong attention to detail
Leadership: Proven ability to lead teams and collaborate across functions
Adaptability: Self-driven and comfortable working in dynamic, global environments
Business Acumen: Ability to combine strategic thinking with practical execution
Technical Skills: Familiarity with data analysis tools
Industry Exposure: Experience in a technical or regulated industry is advantageous
Communication: Strong written and verbal communication skills

Job Responsibility

Lead teams in delivering multi-market research initiatives and data-driven projects
Define project scope, including analytical approach, research methodology, timelines and deliverables
Ensure projects are executed efficiently and aligned with stakeholder expectations
Identify opportunities to enhance existing solutions and develop new analytical approaches
Apply advanced analytical techniques to generate meaningful business insights
Deliver high-quality insights with strong subject-matter understanding across assigned sectors or regions
Translate complex data into clear, actionable recommendations
Lead presentations and communicate findings effectively to stakeholders
Act as a key point of contact for project updates and deliverables
Collaborate with stakeholders to ensure outputs meet business needs

Fulltime

Senior Clinical Research Associate/Clinical Research Associate II - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
Preferred therapeutic experience in Oncology
Global clinical trial experience preferred
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Travel (60-80%) within area is required
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites
Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
Provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F)
Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
Partner with SCP and the study team to define and support recruitment initiatives at site level

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Select Country

Associate Research Manager

Requirements

Looking for more opportunities?